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Clinical frailty, and not features of acute infection, is associated with late mortality in COVID-19: a retrospective cohort study.
Vlachogiannis, Nikolaos I; Baker, Kenneth F; Georgiopoulos, Georgios; Lazaridis, Charalampos; van der Loeff, Ina Schim; Hanrath, Aidan T; Sopova, Kateryna; Tual-Chalot, Simon; Gatsiou, Aikaterini; Spyridopoulos, Ioakim; Stamatelopoulos, Kimon; Duncan, Christopher J A; Stellos, Konstantinos.
  • Vlachogiannis NI; Biosciences Institute, Vascular Biology and Medicine Theme, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK.
  • Baker KF; RVI and Freeman Hospitals, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
  • Georgiopoulos G; RVI and Freeman Hospitals, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
  • Lazaridis C; Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK.
  • van der Loeff IS; NIHR Newcastle Biomedical Research Centre, Newcastle University and Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
  • Hanrath AT; Biosciences Institute, Vascular Biology and Medicine Theme, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK.
  • Sopova K; Department of Clinical Therapeutics, National and Kapodistrian University of Athens Medical School, Athens, Greece.
  • Tual-Chalot S; RVI and Freeman Hospitals, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
  • Gatsiou A; Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK.
  • Spyridopoulos I; Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK.
  • Stamatelopoulos K; RVI and Freeman Hospitals, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
  • Duncan CJA; Biosciences Institute, Vascular Biology and Medicine Theme, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK.
  • Stellos K; Biosciences Institute, Vascular Biology and Medicine Theme, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK.
J Cachexia Sarcopenia Muscle ; 13(3): 1502-1513, 2022 06.
Article in English | MEDLINE | ID: covidwho-1729145
ABSTRACT

BACKGROUND:

Coronavirus disease 2019 (COVID-19) is associated with excess mortality after hospital discharge. Identification of patients at increased risk of death following hospital discharge is needed to guide clinical monitoring and early intervention. Herein, we aimed to identify predictors of early vs. late mortality in COVID-19 patients.

METHODS:

A total of 471 patients with polymerase chain reaction-confirmed COVID-19 were followed up for 9 months [median (inter-quartile range) of follow-up time 271 (14) days] after hospital admission. COVID-19-related signs and symptoms, laboratory features, co-morbidities, Coronavirus Clinical Characterisation Consortium (4C) mortality and Clinical Frailty Scale (CFS) scores were analysed by logistic regression for association with early (28 day) vs. late mortality. Receiver operating characteristic (ROC) analysis was used to determine the discriminative value of 4C and CFS scores for early vs. late mortality.

RESULTS:

A total of 120 patients died within 28 days from hospital admission. Of the remaining 351 patients, 41 died within the next 8 months. Respiratory failure, systemic inflammation, and renal impairment were associated with early mortality, while active cancer and dementia were associated with late mortality, after adjustment for age and sex. 4C mortality score and CFS were associated with both early [odds ratio (OR) (95% confidence interval-CI) 4C 1.34 (1.25-1.45); CFS 1.49 (1.33-1.66)] and late [OR (95% CI) 4C 1.23 (1.12-1.36); CFS 2.04 (1.62-2.56)] mortality. After adjustment for CFS, the association between 4C and late mortality was lost. By ROC analysis, 4C mortality score was superior to CFS for 28 day mortality [area under the curve (AUC) (95% CI) 0.779 (0.732-0.825) vs. 0.723 (0.673-0.773), respectively; P = 0.039]. In contrast, CFS had higher predictive value for late mortality compared with 4C mortality score [AUC (95% CI) 0.830 (0.776-0.883) vs. 0.724 (0.650-0.798), respectively; P = 0.007].

CONCLUSIONS:

In our cohort, late mortality in COVID-19 patients is more strongly associated with premorbid clinical frailty than with severity of the acute infection phase.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Fatigue Syndrome, Chronic / Frailty / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: J Cachexia Sarcopenia Muscle Year: 2022 Document Type: Article Affiliation country: Jcsm.12966

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Fatigue Syndrome, Chronic / Frailty / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: J Cachexia Sarcopenia Muscle Year: 2022 Document Type: Article Affiliation country: Jcsm.12966